Večerić-Haler Željka, Bizjak Boštjan, Romozi Karmen, Arnol Miha
Clin Nephrol. 2017;88(13):126-130. doi: 10.5414/CNP88FX27.
The aim of this study was to compare the efficacy and safety of two subsequent CMV prophylaxis regimens for prevention of cytomegalovirus (CMV) infection and disease in our kidney transplant recipients (KTRs).
In an historic-cohort of KTRs, two CMV prophylaxis protocols were compared: short protocol in which CMV IgG seronegative recipients (R-) of CMV IgG seropositive donors (D+) received valganciclovir for 3 months post-transplant (group 1: 2005 - 2010); and expanded protocol in which prophylaxis for high-risk recipients was extended to 6 months, and a 3-month prophylaxis for D+/R+ and D-/R+ was introduced (group 2: 2011 - 2016). Incidences of CMV viremia, disease, and adverse events were assessed 12 months after transplant.
Of 457 KTRs, 167 received short (group 1) and 290 expanded (group 2) CMV prophylaxis. The incidence of CMV viremia was significantly lower in group 2 than in group 1: 17.6% vs. 29.2%, respectively (p = 0.001). The incidence of CMV disease was 5.2% in group 2 vs. 10.2% in group 1 (p = 0.04). After comparing group 2 and group 1 according to the risk of CMV infection, incidences of CMV viremia were 50% vs. 47.4% in D+/R- (p = 0.79), 3.1% vs. 5.7% in D-/R+ (p = 0.05), and 9.7% vs. 23.6% in D+/R+ (p = 0.0004). The incidence of neutropenia was 41.7% in group 2 and 33.5% in group 1 (p = 0.09).
CONCLUSIONS: The results show a significant reduction of CMV viremia in D+/R+ and D-/R+ KTRs after introduction of 3-month prophylaxis with valganciclovir. Extension of CMV prophylaxis to 6 months in D+/R- was not associated with reduction in CMV viremia at 12 months after transplant. .
本研究旨在比较两种连续的巨细胞病毒(CMV)预防方案在预防肾移植受者(KTRs)巨细胞病毒感染和疾病方面的疗效和安全性。
在一个KTRs的历史性队列中,比较了两种CMV预防方案:短期方案,即CMV IgG血清学阴性受者(R-)接受CMV IgG血清学阳性供者(D+)的肾移植后,接受缬更昔洛韦治疗3个月(第1组:2005 - 2010年);扩展方案,即高危受者的预防时间延长至6个月,并引入对D+/R+和D-/R+受者进行3个月的预防(第2组:2011 - 2016年)。在移植后12个月评估CMV病毒血症、疾病和不良事件的发生率。
457例KTRs中,167例接受短期(第1组)CMV预防,290例接受扩展(第2组)CMV预防。第2组CMV病毒血症的发生率显著低于第1组,分别为17.6%和29.2%(p = 0.001)。第2组CMV疾病的发生率为5.2%,第1组为10.2%(p = 0.04)。根据CMV感染风险比较第2组和第1组后,D+/R-中CMV病毒血症的发生率分别为50%和47.4%(p = 0.79),D-/R+中为3.1%和5.7%(p = 0.05),D+/R+中为9.7%和23.6%(p = 0.0004)。第2组中性粒细胞减少的发生率为41.7%,第1组为33.5%(p = 0.09)。
结果显示,在引入缬更昔洛韦3个月预防后,D+/R+和D-/R+ KTRs的CMV病毒血症显著降低。将D+/R-受者的CMV预防延长至6个月与移植后12个月时CMV病毒血症的降低无关。